Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K822385Substantially Equivalent

Extrapure Reverse Osmosis Water Unit

Extracorporeal Medical Specialities, Inc., Mchenry IL / Traditional, Substantially Equivalent

K822385 is the FDA 510(k) clearance record for EXTRAPURE REVERSE OSMOSIS WATER UNIT, a class II device, cleared for Extracorporeal Medical Specialities, Inc. on under FDA product code FIP (Subsystem, Water Purification). FDA records list 69 510(k) clearances for Extracorporeal Medical Specialities, Inc., from to . As of , FDA records show no recalls naming K822385.

Clearance record

Decision date
Received
(65 days to decision)
Product code
FIP Subsystem, Water Purification
Regulation
21 CFR 876.5665
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Extracorporeal Medical Specialities, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FIP

Trailing 12 months
1 clearance under product code FIP in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FIP, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260